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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380329Generated: November 4, 2026

Sodium borohydride → HCID 70434749, compound

https://huagongshe.com/reaction/1380329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20214926HCID 20214926—
ReactantHCID 20214946HCID 20214946—
SolventMethanolHCID 887—
ProductHCID 70434749HCID 7043474950.4%

Reaction Steps

A mixture of 9.3 gm of 2,5-dichloro-4-hydroxyphenyl-glyoxal hydrate, 7.25 gm of 1-(3-amino-3-methylbutyl)-benzimidazole and 100 ml of alcohol was stirred for 3 hours at 40°-45° C. The resulting solution was subsequently cooled, admixed in portions with 8 gm of sodium borohydride, and the mixture was stirred for 3 hours at room temperature. After the addition of 100 ml of methanol for decomposition of the sodium borohydride, the mixture was allowed to stand for 10 hours, the solvent was distilled off under reduced pressure, the residue was dissolved in 200 ml of water, and the solution was acidified with concentrated hydrochloric acid. 9.5 gm of 1-(2,5-dichloro-4-hydroxyphenyl)-2-[4-(1-benzimidazolyl)-2-methyl-2-butylamino]-ethanol dihydrochloride×1H2O, m.p. 180°-183° C., of the formula ##STR29## were obtained. The yield was 50.4% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581367
Source datasetuspto-grants-1986_04
ORD IDord-e6b474f54bb04834a8bd2b8216c7938e
Source noteuspto-grants-1986_04